Effect of magnesium on reducing the UV-induced oxidative damage in marrow mesenchymal stem cells

被引:17
作者
Chen, Yangmei [1 ,2 ,3 ]
Xiong, Shibing [1 ,2 ,3 ]
Zhao, Fenghua [1 ,2 ,3 ]
Lu, Xugang [1 ,2 ,3 ]
Wu, Boyao [1 ,2 ,3 ]
Yang, Bangcheng [1 ,2 ,3 ,4 ]
机构
[1] Sichuan Univ, Engn Res Ctr Biomat, Chengdu 610064, Sichuan, Peoples R China
[2] Natl Engn Res Ctr Biomat, Chengdu 610064, Sichuan, Peoples R China
[3] Sichuan Guojia Biomat Co Ltd, Chengdu 610064, Sichuan, Peoples R China
[4] Nanjing Normal Univ, Jiangsu Collaborat Innovat Ctr Biomed Funct Mat, Nanjing 210046, Jiangsu, Peoples R China
关键词
magnesium; UV radiation; oxidative stress damage; mitochondria; cell apoptosis; OXYGEN SPECIES ROS; BCL-2 FAMILY PROTEINS; REACTIVE OXYGEN; MITOCHONDRIAL DYSFUNCTION; STRESS DAMAGE; DEATH; RESPONSES; ANTIOXIDANT; AUTOPHAGY; DISEASE;
D O I
10.1002/jbm.a.36634
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Oxidative stress could cause damage to lipids, proteins and DNA, which is induced by the imbalance between the production of reactive oxygen species (ROS) and the biological system ability to counteract or detoxify their harmful effects. The oxidative stress damage significantly contributes to a number of diseases. Magnesium (Mg) is endowed with a novel function of removing excess ROS by releasing H-2 during the degradation. In this study, in order to explore the property of anti-oxidative damage of Mg metal, rat bone marrow mesenchymal stem cells (MSCs) oxidative damaged by ultraviolet (UV) radiation was employed to co-culture with Mg metal. The effect of Mg metal on the response of antioxidant enzymes and mitochondria in MSCs was studied. We found that Mg metal could reduce the cellular oxidative stress damage and elevate the activities of antioxidant enzymes to maintain redox homeostasis. In addition, Mg metal could reduce the risk of UV-induced cell apoptosis by increasing the ratio of Bcl-2/Bax, elevating the mitochondrial membrane potential and blocking the release of cytochrome c. This finding showed Mg metal might have the potential for treating diseases caused by oxidative stress damage. (c) 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 107A: 1253-1263, 2019.
引用
收藏
页码:1253 / 1263
页数:11
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